A kind of bifunctional starch-based composite nanoparticle and its preparation method and application
A composite nanoparticle and functional technology, applied in the field of starch deep processing, can solve the problems of poor stability of double emulsion and limited industrial application.
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[0050] One aspect of the embodiments of the present invention provides a method for preparing bifunctional starch-based composite nanoparticles, which includes:
[0051] Perform hydrolysis treatment on starch to form starch hydrolyzate and obtain linear dextrin;
[0052] The linear dextrin is classified by an alcohol-alcohol gradient precipitation method to obtain a linear dextrin with uniform molecular weight distribution;
[0053] Oxidizing the linear dextrin by using a TEMPO / NaClO / NaBr oxidation system to obtain oxidized dextrin;
[0054] making the first mixed system comprising oxidized dextrin and curcumin undergo a complex reaction to form an oxidized dextrin-curcumin complex; and,
[0055] Make the oxidized dextrin-curcumin complex and chitosan hydrochloride form oxidized dextrin-curcumin / chitosan hydrochloride composite nanoparticles through electrostatic complexation to obtain the bifunctional starch-based composite nanoparticles.
[0056] In some embodiments, the ...
Embodiment 1
[0138] 1) Preparation of linear dextrin (LD)
[0139] 20g of ordinary cornstarch is configured into starch milk with a mass fraction of 5wt%, placed in a boiling water bath and stirred for 1h to completely gelatinize the starch, and further place the gelatinized starch in an acetate solution (0.02mol / L, with a pH of 6) Add 80U α-amylase, carry out hydrolysis treatment at 60°C for 1.5h, heat up to 100°C for enzyme inactivation treatment, add 1000U pullulanase for debranching treatment at 55°C for 3h, after the reaction, put the reaction solution in Inactivate the enzyme in a boiling water bath for 10 minutes. The reactant was centrifuged at 4500 g for 20 min, the precipitate was discarded, the supernatant was subjected to rotary evaporation, and vacuum freeze-dried to obtain linear dextrin.
[0140] 2) Grading of linear dextrins
[0141] LDs were fractionated by alcohol-alcohol precipitation gradient precipitation. Briefly, absolute ethanol was slowly added to the LD dispers...
Embodiment 2
[0154] 1) Preparation of linear dextrin (LD)
[0155] 20g waxy corn starch is configured into starch milk with a mass fraction of 5wt%, placed in a boiling water bath and stirred for 1h to completely gelatinize the starch, and further place the gelatinized starch in an acetate solution (0.02mol / L, pH = 6) Add 40U α-amylase, perform hydrolysis treatment at 50°C for 2 hours, heat up to 110°C for enzyme inactivation treatment, add 600U pullulanase for debranching treatment for 3.5 hours after cooling to 60°C, and place the reaction solution in the Inactivate the enzyme in a boiling water bath for 15 minutes. The reactant was centrifuged at 4500 g for 20 min, the precipitate was discarded, the supernatant was subjected to rotary evaporation, and vacuum freeze-dried to obtain linear dextrin.
[0156] 2) Grading of linear dextrins
[0157] LDs were fractionated by alcohol-alcohol precipitation gradient precipitation. In brief, absolute ethanol was slowly added to the LD dispersio...
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